Case of ovarian dysgenesis and dilated cardiomyopathy supports existence of malouf syndrome
- 1 October 1992
- journal article
- case report
- Published by Wiley in American Journal of Medical Genetics
- Vol. 44 (3), 369-373
- https://doi.org/10.1002/ajmg.1320440320
Abstract
We describe an 18-year-old girl with ovarian dysgenesis, dilated cardiomyopathy, mild mental retardation, broad nasal base, blepharoptosis, and minor skeletal abnormalities. This unusual association of manifestations was first reported by Malouf et al. [1985]. Our patient, although a sporadic case, supports the existence of Malouf syndrome.Keywords
This publication has 10 references indexed in Scilit:
- Sudden death in hypertrophic cardiomyopathy associated with 46,XY pure gonadal dysgenesisAmerican Heart Journal, 1988
- Late onset dilated cardiomyopathy in a unique familial syndrome of hypogonadism and metabolic abnormalitiesAmerican Heart Journal, 1987
- Hypergonadotropic hypogonadism with congestive cardiomyopathyAmerican Journal of Medical Genetics, 1987
- Noonan syndrome: A reviewAmerican Journal of Medical Genetics, 1985
- Hypergonadotropic hypogonadism with congestive cardiomyopathy: An autosomal‐recessive disorder?American Journal of Medical Genetics, 1985
- Genital anomaly and cardiomyopathy: a new syndromeClinical Genetics, 1984
- Obstructive Cardiomyopathy in a Male Dwarf with CryptorchidismClinical Cardiology, 1982
- Familial Cardiomyopathy, Hypogonadism, and CollagenomaAnnals of Internal Medicine, 1980
- The perrault syndrome: Autosomal recessive ovarian dysgenesis with facultative, non‐sex‐limited sensorineural deafnessAmerican Journal of Medical Genetics, 1979
- Genital anomaly, mental retardation, and cardiomyopathy: A new syndrome?The Journal of Pediatrics, 1973